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Identification and analysis for cross-reactivity among hantaviruses of H-2b-restricted cytotoxic T-lymphocyte epitopes in Sin Nombre virus nucleocapsid protein

机译:sin Nombre病毒核衣壳蛋白中H-2b限制性细胞毒性T淋巴细胞表位汉坦病毒交叉反应的鉴定与分析

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摘要

Sin Nombre virus (SNV) causes hantavirus pulmonary syndrome (HPS), with a high rate of mortality in humans who are infected by the transmission of virus from the natural rodent host. In humans, cytotoxic T lymphocytes (CTL) specific for SNV appear to play an important role in the pathogenicity of HPS. There is a correlation between the frequencies of SNV-specific CTLs and the severity of HPS disease. In order to create a mouse model to study the role of SNV-specific T cells in vivo, T cell responses to SNV nucleocapsid (N) protein in B6.PL Thy1(a)/Cy mice (H-2(b)) immunized with plasmid DNA or recombinant vaccinia virus expressing SNV N protein were examined. Four peptides, NC94-101, NC175-189, NC217-231 and NC331-345, were recognized by CD8(+) T cells in CTL and ELISPOT assays in SNV N-immunized mice. Interestingly, two of these epitopes are located in the central region of the SNV N protein, where several human CD8(+) T-cell epitopes have been defined in Puumala virus and SNV. CTL lines specific for these four epitopes were cross-reactive to corresponding Puumala virus peptides, but only one of them was cross-reactive to Hantaan virus peptides. These results will enable the analysis of the roles of CTL in immunopathology of HPS in experimental mouse models of HPS.
机译:罪孽病毒(SNV)导致汉坦病毒性肺综合症(HPS),在被天然啮齿动物宿主传播的病毒感染的人类中,死亡率很高。在人类中,SNV特异的细胞毒性T淋巴细胞(CTL)似乎在HPS的致病性中起重要作用。 SNV特异性CTL的频率与HPS疾病的严重程度之间存在相关性。为了创建小鼠模型来研究SNV特异性T细胞在体内的作用,在免疫B6.PL Thy1(a)/ Cy小鼠(H-2(b))中,T细胞对SNV核衣壳(N)蛋白的反应用表达SNV N蛋白的质粒DNA或重组痘苗病毒检测了病毒。在SNV N免疫小鼠的CTL和ELISPOT分析中,CD8(+)T细胞可识别四种肽NC94-101,NC175-189,NC217-231和NC331-345。有趣的是,这些表位中的两个位于SNV N蛋白的中心区域,在Puumala病毒和SNV中已定义了几个人CD8(+)T细胞表位。对这四个表位具有特异性的CTL谱系与相应的Puumala病毒肽具有交叉反应性,但其中只有一个与汉坦病毒肽具有交叉反应性。这些结果将能够分析HPS实验小鼠模型中CTL在HPS免疫病理学中的作用。

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